A proteomic approach to the identification of early molecular targets changed by L-ascorbic acid in NB4 human leukemia cells
✍ Scribed by Seyeon Park; Joomin Lee; Chang-Hwan Yeom
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 424 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0730-2312
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✦ Synopsis
Abstract
The pro‐oxidant effect of L‐ascorbic acid (LAA) is toxic to leukemia cells. LAA induces the oxidation of glutathione to its oxidized form (GSSG) and this is followed by a concentration‐dependent H~2~O~2~ accumulation, which occurs in parallel to the induction of apoptosis. To identify early protein targets of LAA in leukemia cells, we used a differential proteomics approach in NB4 human leukemia cells treated with 0.5 mM of LAA for 30 min. This exposure was determined to efficiently block cellular proliferation and to activate oxidative stress‐inducible apoptosis. We identified nine proteins that sensitively reacted to LAA treatment by using two‐dimensional (2‐D) gel electrophoresis and matrix‐assisted laser desorption ionization time‐of‐flight‐MS. A subunit of protein‐disulfide isomerase (a thiol/disulfide exchange catalyst) and immunoglobulin‐heavy‐chain binding protein (BiP, identical to Hsp70 chaperone) showed quantitative expression profile differences. A myeloid leukemia associated antigen protein (a tropomyosin isoform) showed changes in pI as a result of phosphorylation. Our studies demonstrate for the first time that the addition of LAA to cells results in an immediate change in the intracellular thiol/disulfide condition and that this includes an increase in the GSH oxidation with changes in the superfamily of thiol/disulfide exchange catalysts. These results suggest that LAA oxidizes intracellular reduced glutathione and modulates disulfide bond formation in proteins. J. Cell. Biochem. 99: 1628–1641, 2006. © 2006 Wiley‐Liss, Inc.